Literature DB >> 27562064

Rare phenotypes in the understanding of autoimmunity.

Yvonne Zeissig1, Britt-Sabina Petersen2, Andre Franke2, Richard S Blumberg3, Sebastian Zeissig4,5.   

Abstract

The study of rare phenotypes has a long history in the description of autoimmune disorders. First Mendelian syndromes of idiopathic tissue destruction were defined more than 100 years ago and were later revealed to result from immune-mediated reactivity against self. In the past two decades, continuous advances in sequencing technology and particularly the advent of next-generation sequencing have allowed to define the genetic basis of an ever-growing number of Mendelian forms of autoimmunity. This has provided unique insight into the molecular pathways that govern immunological homeostasis and that are indispensable for the prevention of self-reactive immune-mediated tissue damage and 'horror autotoxicus'. Here we will discuss selected examples of past and recent investigations into rare phenotypes of autoimmunity that have delineated pathways critical for central and peripheral control of the adaptive immune system. We will outline the implications of these findings for rare and common forms of autoimmunity and will discuss the benefits and potential pitfalls of the integration of next-generation sequencing into algorithms for clinical diagnostics. Because of the concise nature of this review, we will focus on syndromes caused by defects in the control of adaptive immunity as innate immune-mediated autoinflammatory disorders have been covered in excellent recent reviews on Mendelian and polygenic forms of autoimmunity.

Entities:  

Mesh:

Year:  2016        PMID: 27562064      PMCID: PMC5371426          DOI: 10.1038/icb.2016.76

Source DB:  PubMed          Journal:  Immunol Cell Biol        ISSN: 0818-9641            Impact factor:   5.126


  82 in total

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Journal:  Nat Immunol       Date:  2003-03-03       Impact factor: 25.606

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Journal:  Cell       Date:  1993-10-22       Impact factor: 41.582

9.  Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4.

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Journal:  Science       Date:  1995-11-10       Impact factor: 47.728

10.  X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.

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Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

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